A method for performing an empirical test for the presence of bi-modal data

• 1. 对存在码间干扰并在多路发送和接收中进行按位交织编码的数字数据流进行编码/解码的方法及相应系统 [P] . 中国专利： CN1310458C . 2007.04.11
• 2. 对存在码间干扰并在多路发送和接收中进行按位交织编码的数字数据流进行编码/解码的方法及相应系统 [P] . 中国专利： CN1507714A . 2004-06-23
• 3. Method for performing an empirical test for the presence of bi-modal data [P] . 美国专利： US7136809B2 . 2006-11-14

  机译： 对存在双峰数据进行经验检验的方法

• 4. A method for performing an empirical test for the presence of bi-modal data [P] . 欧洲知识产权局专利： EP1416438A2 . 2004-05-06

  机译： 一种对存在双峰数据进行经验检验的方法

• 5. Method for performing an empirical test for the presence of bi-modal data [P] . 美国专利： US2004088159A1 . 2004-05-06

  机译： 对双峰数据进行实证检验的方法

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• 2. Testing a Four-Dimensional Variational Data Assimilation Method Using an Improved Intermediate Coupled Model for ENSO Analysis and Prediction [J] . Chuan GAO, Xinrong WU, Rong-Hua ZHANG 大气科学进展（英文版） . 2016,第007期
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• 6. The bacterial identification and antimicrobial susceptibility testing are usually performed manually. Recently, the number of samples has increased and the need for automatification has grown. BioMerieux has investigated Vitek2 for this purpose. HUSLAB has assigned us to compare the identification and antimicrobial results with respect to routine methods and Vitek2. Furthermore, we evaluate test reactions, ESBL (Extended Spectrum Beta-Lactamase) production and the time what it takes to get results with Vitek2. In this study, we examined a total of 183 bacterial isolates including 76 ESBL-strains, 40 nonfermenting rods, 41 fastidious bacteria and 26 fresh clinical isolates. The results of routine methods were gathered from the patient database and following this, compared to the results given by Vitek2. Vitek2 correctly identified more than 96 f the ESBL-strains and fresh clinical isolates. The results of nonfermenting rods and fastidious bacteri a were 70 oncordant with those of the routine methods. Test reaction results of Api20E were 94 nd Api20NE 70 n concordance with Vitek2 results. Approximately 80 f all Vitek2 antimicrobial results and 90 f ESBL test results were correct. Compared to earlier studies, Vitek2 performed the tests faster than the routine methods. These results suggest that Vitek2 is capable of giving rapid and accurate results. However, nonfermenting rods and fastidious bacteria should be studied further. [O] . Järveläinen Marika, Roslund Iira, Silander Maarit 2006
• 7. A FORTRAN Computer Program to Perform Goodness of Fit Testing on Empirical Data. [R] . Guthrie, S. D. 1979

• 1. Data Consistency Tests through the Use of Neural Networks and Virial Equation. Application of the Proposed Methodology to Critical Study of Density Data [J] . Abdeslam Hassen Meniai ,Serge Laugier ,Hakim Madani . 物理化学期刊（英文） . 2011,第3期
• 2. MODIS BRIGHTNESS TEMPERATURE DATA ASSIMILATION UNDER CLOUDY CONDITIONS: METHODS AND IDEAL TESTS [J] . 丁伟钰 ,万齐林 ,张诚忠 . 热带气象学报：英文版 . 2010,第4期
• 3. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
• 4. 一种模拟变电站运行状态进行全站交流二次回路检验方法研究 [C] . 刘柱揆 ,许守东 ,周鑫 . 2012年云南电力技术论坛 . 2012
• 5. 患者样本数据进行常规免疫定量检验室内质量控制方法的建立与应用 [A] . 程成全 . 2020